Welcome to LookChem.com Sign In|Join Free
  • or
6-dimethylaminomethyl-2-methoxy-4-allylphenol is a complex organic compound with the molecular formula C13H19NO2. It is characterized by a phenol core, which is a benzene with ring a hydroxyl group attached. The compound features a 6-dimethylaminomethyl group, which is a methylamine group with two additional methyl groups, attached to the 6th carbon of the phenol ring. Additionally, it has a 2-methoxy group, which is a methoxy group (an ether derivative of methanol) attached to the 2nd carbon, and a 4-allyl group, which is a propene chain (allyl) attached to the 4th carbon. This chemical structure endows the compound with unique properties and potential applications in various fields, such as pharmaceuticals or chemical research.

1952-82-5

Post Buying Request

1952-82-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1952-82-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1952-82-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1952-82:
(6*1)+(5*9)+(4*5)+(3*2)+(2*8)+(1*2)=95
95 % 10 = 5
So 1952-82-5 is a valid CAS Registry Number.

1952-82-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-dimethylaminomethyl-2-methoxy-4-allylphenol

1.2 Other means of identification

Product number -
Other names 4-Allyl-6-dimethylaminomethyl-2-methoxy-phenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1952-82-5 SDS

1952-82-5Relevant academic research and scientific papers

Phenolic structure and colour in Mannich reaction products

Tyman, John H.P.,Patel, Mahesh

, p. 34 - 37 (2008/02/02)

Mannich reactions have been carried out with a variety of model alkylphenols and dimethylamine, methylamine, and diethylenetriamine to trace the origin of persistent coloured products occurring in related reactions with pentadeca(e)nylphenol and 4-tert-alkylphenols. It was found to be attributable to the presence of resorcinolic impurities.

Synthesis of the β2 Agonist (R)-Salmeterol Using a Sequence of Supported Reagents and Scavenging Agents

Bream, Robert N.,Ley, Steven V.,Procopiou, Panayiotis A.

, p. 3793 - 3796 (2007/10/03)

(Matrix Presented) The enantioselective synthesis of (R)-salmeterol has been achieved by using a sequence of supported reagents and sequestering agents. The saligenin core was installed by a regiospecific alkylation and a chiral auxiliary approach was employed to introduce the desired stereochemistry via a diastereoselective reduction.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1952-82-5